Advertisement

Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1

Srinivas Aluri, Rongbao Zhao, Charlotte Lubout, Susanna M. I. Goorden, Andras Fiser and I. David Goldman

Article Information

Citation 
vol. 2 no. 1 61-68
PubMed 

Print ISSN 
Online ISSN 
History 
  • Submitted September 21, 2017
  • Accepted November 28, 2017
  • Published online January 5, 2018.


Contributors 
  • Srinivas Aluri, 1Department of Pharmacology and2Department of Medicine, Albert Einstein College of Medicine, Bronx, NY;
  • Rongbao Zhao, 1Department of Pharmacology and2Department of Medicine, Albert Einstein College of Medicine, Bronx, NY;
  • Charlotte Lubout, 3Department of Pediatrics,4Division of Metabolic Disorders,
  • Susanna M. I. Goorden, 5Department of Clinical Chemistry, and6Laboratory Genetic Metabolic Diseases, Academic Medical Center, University Hospital of Amsterdam, Amsterdam, The Netherlands; and
  • Andras Fiser, 7Department of Biochemistry and8Department of Systems Biology, Albert Einstein College of Medicine, Bronx, NY
  • I. David Goldman, 1Department of Pharmacology and2Department of Medicine, Albert Einstein College of Medicine, Bronx, NY;

Altmetric.com Statistics

The Altmetric score is a weighted count of online attention designed to reflect the volume and reach of online engagement surrounding an individual research output